{"title":"A Short-Term View of Protein Sequence Evolution from Salmonella.","authors":"Joshua L Cherry","doi":"10.1093/gbe/evaf040","DOIUrl":null,"url":null,"abstract":"<p><p>Much of the study of protein sequence evolution is based on sequence changes inferred to have occurred in nature. The sequences compared for this purpose are usually sufficiently distant that purifying selection has had nearly its full effect and most of the changes inferred have been exposed to a variety of conditions. Here, I make use of large numbers of Salmonella genome sequences to study changes known to be of very recent origin because they are inferred from comparison of very closely related sequences. The effects of purifying selection are weak yet discernible on this short timescale: the ratio of nonsynonymous to synonymous changes is smaller than expected under selective neutrality, but only slightly so. Essential genes have lower rates of nonsynonymous change, as they do on a longer timescale, but much more of this association remains after controlling for expression level. Positive selection for nonsynonymous change is inferred for 151 genes. For nearly half of these, this is attributable to selection for loss of function. Other forms of positive selection inferred include selection for amino acid changes that make enzymes less sensitive to antibiotics and selection for activating changes to proteins involved in transcriptional regulation. Positively selected variants of many genes are likely favored only under unusual conditions and disfavored in the long term, making detection of the positive selection with more distant comparisons difficult or impossible. The short-term view provided by close comparisons complements the long-term view obtained from more distant comparisons such as those between species.</p>","PeriodicalId":12779,"journal":{"name":"Genome Biology and Evolution","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11925014/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome Biology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/gbe/evaf040","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Much of the study of protein sequence evolution is based on sequence changes inferred to have occurred in nature. The sequences compared for this purpose are usually sufficiently distant that purifying selection has had nearly its full effect and most of the changes inferred have been exposed to a variety of conditions. Here, I make use of large numbers of Salmonella genome sequences to study changes known to be of very recent origin because they are inferred from comparison of very closely related sequences. The effects of purifying selection are weak yet discernible on this short timescale: the ratio of nonsynonymous to synonymous changes is smaller than expected under selective neutrality, but only slightly so. Essential genes have lower rates of nonsynonymous change, as they do on a longer timescale, but much more of this association remains after controlling for expression level. Positive selection for nonsynonymous change is inferred for 151 genes. For nearly half of these, this is attributable to selection for loss of function. Other forms of positive selection inferred include selection for amino acid changes that make enzymes less sensitive to antibiotics and selection for activating changes to proteins involved in transcriptional regulation. Positively selected variants of many genes are likely favored only under unusual conditions and disfavored in the long term, making detection of the positive selection with more distant comparisons difficult or impossible. The short-term view provided by close comparisons complements the long-term view obtained from more distant comparisons such as those between species.
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About the journal
Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.